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10.1038/s41467-020-18880-0

http://scihub22266oqcxt.onion/10.1038/s41467-020-18880-0
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33057007!7560817!33057007
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suck abstract from ncbi


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pmid33057007      Nat+Commun 2020 ; 11 (1): 5165
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  • ACE2 mouse models: a toolbox for cardiovascular and pulmonary research #MMPMID33057007
  • Jia H; Yue X; Lazartigues E
  • Nat Commun 2020[Oct]; 11 (1): 5165 PMID33057007show ga
  • Angiotensin-converting enzyme 2 (ACE2) has been identified as the host entry receptor for the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) responsible for the COVID-19 pandemic. ACE2 is a regulatory enzyme of the renin-angiotensin system and has protective functions in many cardiovascular, pulmonary and metabolic diseases. This review summarizes available murine models with systemic or organ-specific deletion of ACE2, or with overexpression of murine or human ACE2. The purpose of this review is to provide researchers with the genetic tools available for further understanding of ACE2 biology and for the investigation of ACE2 in the pathogenesis and treatment of COVID-19.
  • |*Disease Models, Animal[MESH]
  • |Angiotensin-Converting Enzyme 2[MESH]
  • |Animals[MESH]
  • |Betacoronavirus/physiology[MESH]
  • |COVID-19[MESH]
  • |Cardiovascular Diseases/metabolism/*pathology[MESH]
  • |Coronavirus Infections/metabolism/pathology/virology[MESH]
  • |Humans[MESH]
  • |Lung Diseases/metabolism/*pathology[MESH]
  • |Metabolic Diseases/metabolism/pathology[MESH]
  • |Mice[MESH]
  • |Mice, Mutant Strains[MESH]
  • |Pandemics[MESH]
  • |Peptidyl-Dipeptidase A/genetics/*metabolism[MESH]
  • |Pneumonia, Viral/metabolism/pathology/virology[MESH]


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